Ubaid Khan

ORCID: 0000-0003-3216-6323
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About
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Research Areas
  • Xenotransplantation and immune response
  • Blood Pressure and Hypertension Studies
  • Intracerebral and Subarachnoid Hemorrhage Research
  • Animal Genetics and Reproduction
  • Acute Ischemic Stroke Management
  • Cardiac pacing and defibrillation studies
  • Neurosurgical Procedures and Complications
  • Cardiac Arrhythmias and Treatments
  • Poxvirus research and outbreaks
  • Venous Thromboembolism Diagnosis and Management
  • Cerebral Venous Sinus Thrombosis
  • Dialysis and Renal Disease Management
  • Heart Failure Treatment and Management
  • Vaccine Coverage and Hesitancy
  • Immunodeficiency and Autoimmune Disorders
  • Atrial Fibrillation Management and Outcomes
  • COVID-19 epidemiological studies
  • Vascular Procedures and Complications
  • Blood disorders and treatments
  • Chemotherapy-induced cardiotoxicity and mitigation
  • Renal and Vascular Pathologies
  • Cardiovascular Health and Risk Factors
  • Thermal Regulation in Medicine
  • Tissue Engineering and Regenerative Medicine
  • High Altitude and Hypoxia

University of Maryland, Baltimore
2024-2025

King Edward Medical University
2021-2024

University of Maryland Medical Center
2024

The George Institute for Global Health
2016

Soochow University
2016

Second Affiliated Hospital of Soochow University
2016

Lahore General Hospital
2008

Abstract Background Wilms tumor (WT) survival has been affected by the evolution in clinical and biological prognostic factors. Significant differences rates indicate need for further efforts to reduce these disparities. This study aims evaluate clinicopathological data impact on among patients after Wilm's diagnosis. Methods The utilized SEERStat Database identify patients, applying software version 8.3.9.2 extraction. Selection criteria involved specific codes based International...

10.1186/s13052-024-01698-7 article EN cc-by ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics 2024-08-06

Bone marrow transplantation (BMT) saves lives in Omenn syndrome, a severe immunodeficiency disorder. Timely genetic diagnosis and matched donor BMT are crucial. Emphasis on newborn screening multidisciplinary care improves outcomes for infants with inherited disorders. Prompt intervention comprehensive management vital successful transplant outcome.

10.1002/ccr3.9295 article EN cc-by Clinical Case Reports 2024-08-01

Omenn syndrome is a rare, autosomal recessive disorder. It disorder that stems from severe combined immunodeficiency in an affected individual. The disease also of rare occurrence children Pakistan because this the age where usually presents, after having developed child. This case report will explore all reasons lead to while reflecting on management profile child.This deals with discussion one such child who was diagnosed Syndrome being several other diseases, which were mistaken for...

10.1016/j.amsu.2022.103319 article EN Annals of Medicine and Surgery 2022-01-28
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